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Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory-Determination of ammonium plus organic nitrogen by a Kjeldahl digestion method and an automated photometric finish that includes digest cleanup by gas diffusion

The National Water Quality Laboratory (NWQL) determined ammonium plus organic nitrogen (Kjeldahl nitrogen) by using semiautomated, block digester methods for filtered and whole-water samples from 1986 until October 1, 1991. During that time, phosphorus was determined by a persulfate digestion method. In 1991, projected increases in demand for both tests by the U.S. Geological Survey?s National Wat
Authors
Charles J. Patton, Earl P. Truitt

Use of field-applied quality control samples to monitor performance of a Goulden large-sample extractor/GC-MS method for pesticides in water

Since 1985, the Goulden large-sample extractor (GLSE) has been used to isolate a broad array of trace-organic contaminants from large volumes of water. In this study, field-applied quality control measures, including matrix and surrogate spikes and blanks, were used to monitor method performance from GLSE extraction through GC-MS analysis. The method was applied to the determination of multiple cl
Authors
W.T. Foreman, Paul M. Gates, G.D. Foster, F. A. Rinella, S. W. McKenzie

Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory-Processing, taxonomy, and quality control of benthic macroinvertebrate samples

Qualitative and quantitative methods to process benthic macroinvertebrate (BMI) samples have been developed and tested by the U.S. Geological Survey?s National Water Quality Laboratory Biological Group. The qualitative processing method is based on visually sorting a sample for up to 2 hours. Sorting focuses on attaining organisms that are likely to result in taxonomic identifications to
Authors
Stephen R. Moulton, James L. Carter, Scott A. Grotheer, Thomas F. Cuffney, Terry M. Short

New reporting procedures based on long-term method detection levels and some considerations for interpretations of water-quality data provided by the U.S. Geological Survey National Water Quality Laboratory

This report describes the U.S. Geological Survey National Water Quality Laboratory's approach for determining long-term method detection levels and establishing reporting levels, details relevant new reporting conventions, and provides preliminary guidance on interpreting data reported with the new conventions. At the long-term method detection level concentration, the risk of a false positive det
Authors
Carolyn J. Oblinger Childress, William T. Foreman, Brooke F. Connor, Thomas J. Maloney

Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory-Determination of arsenic and selenium in water and sediment by graphite furnace atomic absorption spectrometry

Graphite furnace-atomic absorption spectrometry (GF-AAS) is a sensitive, precise, and accurate technique that can be used to determine arsenic and selenium in samples of water and sediment. The GF-AAS method has been developed to replace the hydride generation-atomic absorption spectrometry (HG-AAS) methods because the method detection limits are similar, bias and variability are comparable, and i
Authors
Sandra R. Jones, John R. Garbarino

Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory-Comparison of a nitric acid in-bottle digestion procedure to other whole-water digestion procedures

A hydrochloric acid in-bottle digestion procedure is used to partially digest wholewater samples prior to determining recoverable elements by various analytical methods. The use of hydrochloric acid is problematic for some methods of analysis because of spectral interference. The inbottle digestion procedure has been modified to eliminate such interference by using nitric acid instead of
Authors
John R. Garbarino, Gerald L. Hoffman

US Geological Survey nutrient preservation experiment: Experimental design, statistical analysis, and interpretation of analytical results

This report describes the experimental details and interprets results from a study conducted by the U.S. Geological Survey (USGS) in 1992 to assess the effect of different sample-processing treatments on the stability of eight nutrient species in samples of surface-, ground-, and municipal-supply water during storage at 4 degrees Celsius for about 30 days. Over a 7-week period, splits of filtered-
Authors
Charles J. Patton, Edward J. Gilroy

Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory-Determination of dissolved arsenic, boron, lithium, selenium, strontium, thallium, and vanadium using inductively coupled plasma-mass spectrometry

The inductively coupled plasma-mass spectrometric (ICP-MS) methods have been expanded to include the determination of dissolved arsenic, boron, lithium, selenium, strontium, thallium, and vanadium in filtered, acidified natural water. Method detection limits for these elements are now 10 to 200 times lower than by former U.S. Geological Survey (USGS) methods, thus providing lower variability at am
Authors
John R. Garbarino

Hydraulic and geochemical performance of a permeable reactive barrier containing zero-valent iron, Denver Federal Center

The hydraulic and geochemical performance of a 366 m long permeable reactive barrier (PRB) at the Denver Federal Center, Denver, Colorado, was evaluated. The funnel and gate system, which was installed in 1996 to intercept and remediate ground water contaminated with chlorinated aliphatic hydrocarbons (CAHs), contained four 12.2 m wide gates filled with zero‐valent iron. Ground water mounding on t
Authors
P. B. McMahon, K. F. Dennehy, Mark W. Sandstrom

Improved method for the determination of nonpurgeable suspended organic carbon in natural water by silver filter filtration, wet chemical oxidation, and infrared spectrometry

Precision and accuracy are reported for the first time for the analysis of nonpurgeable suspended organic carbon by silver membrane filtration followed by wet chemical oxidation. A water sample is pressure filtered through a 0.45‐μm‐pore‐size, 47‐mm‐diameter silver membrane filter. The silver membrane filter then is cut into ribbons and placed in a flame‐sealable glass ampule. The organic material
Authors
Mark R. Burkhardt, Ronald W. Brenton, James A. Kammer, Virenda K. Jha, Peggy G. O'Mara-Lopez, Mark T. Woodworth